Marcela A. Michaut

914 total citations
24 papers, 752 citations indexed

About

Marcela A. Michaut is a scholar working on Cell Biology, Physiology and Molecular Biology. According to data from OpenAlex, Marcela A. Michaut has authored 24 papers receiving a total of 752 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cell Biology, 11 papers in Physiology and 9 papers in Molecular Biology. Recurrent topics in Marcela A. Michaut's work include Cellular transport and secretion (15 papers), Erythrocyte Function and Pathophysiology (9 papers) and Microtubule and mitosis dynamics (7 papers). Marcela A. Michaut is often cited by papers focused on Cellular transport and secretion (15 papers), Erythrocyte Function and Pathophysiology (9 papers) and Microtubule and mitosis dynamics (7 papers). Marcela A. Michaut collaborates with scholars based in Argentina, United States and Chile. Marcela A. Michaut's co-authors include Luis S. Mayorga, Claudia N. Tomes, Roberto Yunes, Gerardo De Blas, Pablo E. Visconti, Oscar D. Bello, Alberto Darszon, Claudia L. Treviño, Mitsunori Fukuda and Gerardo A. De Blas and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Marcela A. Michaut

23 papers receiving 746 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marcela A. Michaut Argentina 14 364 336 336 307 129 24 752
Veerle Vanderheyden Belgium 8 428 1.2× 170 0.5× 127 0.4× 191 0.6× 48 0.4× 8 681
M. Natalia Zanetti Argentina 10 217 0.6× 146 0.4× 125 0.4× 113 0.4× 52 0.4× 11 382
Nicola Winston United States 19 817 2.2× 324 1.0× 525 1.6× 1.0k 3.3× 30 0.2× 38 1.6k
Elke Vermassen Belgium 10 420 1.2× 143 0.4× 102 0.3× 153 0.5× 23 0.2× 11 647
Mary Jo Carabatsos United States 9 786 2.2× 288 0.9× 589 1.8× 1.2k 3.9× 18 0.1× 10 1.5k
Baptiste Rode United Kingdom 9 232 0.6× 46 0.1× 171 0.5× 146 0.5× 158 1.2× 15 511
Ruby Chen United States 6 354 1.0× 148 0.4× 262 0.8× 525 1.7× 8 0.1× 10 723
Mark E. Ireland United States 15 459 1.3× 140 0.4× 80 0.2× 54 0.2× 58 0.4× 29 600
Jay Wright United States 12 256 0.7× 95 0.3× 137 0.4× 113 0.4× 83 0.6× 22 532
Sarah E. Fiedler United States 12 219 0.6× 29 0.1× 187 0.6× 185 0.6× 36 0.3× 16 522

Countries citing papers authored by Marcela A. Michaut

Since Specialization
Citations

This map shows the geographic impact of Marcela A. Michaut's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marcela A. Michaut with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcela A. Michaut more than expected).

Fields of papers citing papers by Marcela A. Michaut

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marcela A. Michaut. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marcela A. Michaut. The network helps show where Marcela A. Michaut may publish in the future.

Co-authorship network of co-authors of Marcela A. Michaut

This figure shows the co-authorship network connecting the top 25 collaborators of Marcela A. Michaut. A scholar is included among the top collaborators of Marcela A. Michaut based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marcela A. Michaut. Marcela A. Michaut is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Zanetti, M. Natalia, et al.. (2021). VAMPs sensitive to tetanus toxin are required for cortical granule exocytosis in mouse oocytes. Experimental Cell Research. 405(1). 112629–112629. 3 indexed citations
4.
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Velásquez, Zahady D., Rosa I. Muñoz, Yimo Lin, et al.. (2017). α-SNAP is expressed in mouse ovarian granulosa cells and plays a key role in folliculogenesis and female fertility. Scientific Reports. 7(1). 11765–11765. 12 indexed citations
6.
Bello, Oscar D., M. Natalia Zanetti, Mitsunori Fukuda, et al.. (2016). Rab3A, a possible marker of cortical granules, participates in cortical granule exocytosis in mouse eggs. Experimental Cell Research. 347(1). 42–51. 17 indexed citations
7.
Bello, Oscar D., et al.. (2015). Cortical Granule Exocytosis Is Mediated by Alpha-SNAP and N-Ethilmaleimide Sensitive Factor in Mouse Oocytes. PLoS ONE. 10(8). e0135679–e0135679. 17 indexed citations
8.
Bennett, J., et al.. (2013). MARCKS Protein Is Phosphorylated and Regulates Calcium Mobilization during Human Acrosomal Exocytosis. PLoS ONE. 8(5). e64551–e64551. 13 indexed citations
9.
Bello, Oscar D., M. Natalia Zanetti, Luis S. Mayorga, & Marcela A. Michaut. (2012). RIM, Munc13, and Rab3A interplay in acrosomal exocytosis. Experimental Cell Research. 318(5). 478–488. 35 indexed citations
10.
Bátiz, Luis Federico, Gerardo A. De Blas, Marcela A. Michaut, et al.. (2009). Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction. PLoS ONE. 4(3). e4963–e4963. 24 indexed citations
11.
Michaut, Marcela A., et al.. (2007). Calmodulin and CaMKII in the Sperm Principal Piece: Evidence for a Motility‐Related Calcium/Calmodulin Pathway. Journal of Andrology. 28(5). 706–716. 57 indexed citations
12.
Roggero, Carlos M., Claudia N. Tomes, Gerardo A. De Blas, et al.. (2005). Protein kinase C-mediated phosphorylation of the two polybasic regions of synaptotagmin VI regulates their function in acrosomal exocytosis. Developmental Biology. 285(2). 422–435. 25 indexed citations
13.
Michaut, Marcela A., Carmen J. Williams, & Richard M. Schultz. (2005). Phosphorylated MARCKS: A novel centrosome component that also defines a peripheral subdomain of the cortical actin cap in mouse eggs. Developmental Biology. 280(1). 26–37. 34 indexed citations
14.
Tomes, Claudia N., et al.. (2004). α-SNAP and NSF are required in a priming step during the human sperm acrosome reaction. Molecular Human Reproduction. 11(1). 43–51. 54 indexed citations
15.
Tomes, Claudia N., Marcela A. Michaut, Gerardo De Blas, et al.. (2002). SNARE Complex Assembly Is Required for Human Sperm Acrosome Reaction. Developmental Biology. 243(2). 326–338. 83 indexed citations
16.
Blas, Gerardo De, Marcela A. Michaut, Claudia L. Treviño, et al.. (2002). The Intraacrosomal Calcium Pool Plays a Direct Role in Acrosomal Exocytosis. Journal of Biological Chemistry. 277(51). 49326–49331. 110 indexed citations
17.
Yunes, Roberto, Claudia N. Tomes, Marcela A. Michaut, et al.. (2002). Rab3A and calmodulin regulate acrosomal exocytosis by mechanisms that do not require a direct interaction. FEBS Letters. 525(1-3). 126–130. 26 indexed citations
18.
Michaut, Marcela A., Gerardo De Blas, Claudia N. Tomes, et al.. (2001). Synaptotagmin VI Participates in the Acrosome Reaction of Human Spermatozoa. Developmental Biology. 235(2). 521–529. 61 indexed citations
19.
Yunes, Roberto, Marcela A. Michaut, Claudia N. Tomes, & Luis S. Mayorga. (2000). Rab3A Triggers the Acrosome Reaction in Permeabilized Human Spermatozoa1. Biology of Reproduction. 62(4). 1084–1089. 80 indexed citations
20.
Michaut, Marcela A., Miguel Carrasco, & María S. Giménez. (1992). Effects of Castration on the Content and Labelling of Lipids in Male Rat Liver. Hormone and Metabolic Research. 24(12). 593–594. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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